Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126213921 | 12621392 | 1 | I | 20160801 | 0 | 20160803 | 20160803 | DIR | 58.50 | YR | M | N | 85.70000 | KG | 20160801 | N | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126213921 | 12621392 | 1 | PS | CISPLATIN. | CISPLATIN | 1 | 0 | 212 | MG | ||||||||||
| 126213921 | 12621392 | 3 | SS | IFOSFAMIDE. | IFOSFAMIDE | 1 | 0 | 12780 | MG | ||||||||||
| 126213921 | 12621392 | 4 | SS | TAXOL | PACLITAXEL | 1 | 0 | 533 | MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126213921 | 12621392 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126213921 | 12621392 | Anaemia | |
| 126213921 | 12621392 | Blood creatinine increased | |
| 126213921 | 12621392 | Thrombocytopenia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126213921 | 12621392 | 1 | 20160722 | 0 | ||
| 126213921 | 12621392 | 3 | 20160722 | 0 | ||
| 126213921 | 12621392 | 4 | 20160718 | 0 |